Canonical Allele Identifier: CA388025863

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515219T>A (hg19) ; chr13:g.51941083T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941083T>A , CM000675.2:g.51941083T>A	GRCh38
NC_000013.10:g.52515219T>A , CM000675.1:g.52515219T>A	GRCh37
NC_000013.9:g.51413220T>A	NCBI36
NG_008806.1:g.75412A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1204A>T	ENSP00000489512.2:n.*1204A>T
ENST00000673864.2:c.*2298A>T	ENSP00000501045.2:n.*2298A>T
ENST00000674147.2:c.2933A>T	ENSP00000500964.2:p.Asp978Val
ENST00000242839.10:c.3554A>T MANE Select	ENSP00000242839.5:p.Asp1185Val
ENST00000344297.9:c.2933A>T	ENSP00000342559.5:p.Asp978Val
ENST00000400366.6:c.3221A>T	ENSP00000383217.3:p.Asp1074Val
ENST00000448424.7:c.3302A>T	ENSP00000416738.3:p.Asp1101Val
ENST00000673772.1:c.3320A>T	ENSP00000501168.1:p.Asp1107Val
ENST00000673867.1:n.3693A>T
ENST00000674126.1:n.3917A>T
ENST00000674147.1:c.2489A>T	ENSP00000500964.1:p.Asp830Val
ENST00000242839.8:c.3554A>T	ENSP00000242839.4:p.Asp1185Val
ENST00000344297.8:c.2933A>T	ENSP00000342559.5:p.Asp978Val
ENST00000400366.5:c.3221A>T	ENSP00000383217.3:p.Asp1074Val
ENST00000400370.8:c.2264A>T	ENSP00000383221.3:p.Asp755Val
ENST00000418097.7:c.3359A>T	ENSP00000393343.2:p.Asp1120Val
ENST00000448424.6:c.3320A>T	ENSP00000416738.2:p.Asp1107Val
ENST00000634296.1:c.1332A>T
ENST00000634308.1:c.*655A>T	ENSP00000489234.1:n.*655A>T
ENST00000634620.1:n.4298A>T
ENST00000634810.1:n.2899A>T
ENST00000634844.1:c.3410A>T	ENSP00000489398.1:p.Asp1137Val
NM_000053.3:c.3554A>T	NP_000044.2:p.Asp1185Val
NM_001005918.2:c.2933A>T	NP_001005918.1:p.Asp978Val
NM_001243182.1:c.3221A>T	NP_001230111.1:p.Asp1074Val
XM_005266423.2:c.3458A>T	XP_005266480.1:p.Asp1153Val
XM_005266424.3:c.3458A>T	XP_005266481.1:p.Asp1153Val
XM_005266427.2:c.3320A>T	XP_005266484.1:p.Asp1107Val
XM_005266428.1:c.3302A>T	XP_005266485.1:p.Asp1101Val
XM_005266430.3:c.3554A>T	XP_005266487.1:p.Asp1185Val
XM_005266431.2:c.3518A>T	XP_005266488.1:p.Asp1173Val
XM_005266432.2:c.3068A>T	XP_005266489.1:p.Asp1023Val
XM_006719837.2:c.3458A>T	XP_006719900.1:p.Asp1153Val
XM_006719838.1:c.1370A>T	XP_006719901.1:p.Asp457Val
XM_006719839.1:c.1187A>T	XP_006719902.1:p.Asp396Val
XM_011535117.1:c.3458A>T	XP_011533419.1:p.Asp1153Val
XM_011535118.1:c.3419A>T	XP_011533420.1:p.Asp1140Val
XM_011535119.1:c.3371A>T	XP_011533421.1:p.Asp1124Val
XM_011535120.1:c.3140A>T	XP_011533422.1:p.Asp1047Val
XM_011535121.1:c.3041A>T	XP_011533423.1:p.Asp1014Val
XM_011535122.1:c.2222A>T	XP_011533424.1:p.Asp741Val
XR_941601.1:n.3773A>T
XR_941602.1:n.3773A>T
XR_941603.1:n.3773A>T
XR_941604.1:n.3773A>T
NM_001330578.1:c.3320A>T	NP_001317507.1:p.Asp1107Val
NM_001330579.1:c.3302A>T	NP_001317508.1:p.Asp1101Val
XM_005266424.4:c.3458A>T	XP_005266481.1:p.Asp1153Val
XM_005266430.4:c.3554A>T	XP_005266487.1:p.Asp1185Val
XM_005266431.4:c.3518A>T	XP_005266488.1:p.Asp1173Val
XM_006719837.3:c.3458A>T	XP_006719900.1:p.Asp1153Val
XM_011535117.3:c.3458A>T	XP_011533419.1:p.Asp1153Val
XM_017020627.1:c.3458A>T	XP_016876116.1:p.Asp1153Val
NM_000053.4:c.3554A>T MANE Select	NP_000044.2:p.Asp1185Val
NM_001005918.3:c.2933A>T	NP_001005918.1:p.Asp978Val
NM_001330579.2:c.3302A>T	NP_001317508.1:p.Asp1101Val
NM_001243182.2:c.3221A>T	NP_001230111.1:p.Asp1074Val
NM_001330578.2:c.3320A>T	NP_001317507.1:p.Asp1107Val